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Non-homologous end-joining proteins are required for Agrobacterium T-DNA integration   [0145] 
Genetic requirements for the targeted integration of Agrobacterium T-DNA in Saccharomyces cerevisiae   [0145] 
Involvement of poly(ADP-ribose) polymerase-1 and XRCC1/DNA ligase III in an alternative route for DNA double-strand breaks rejoining   [0145] 
Saccharomyces cerevisiae Ku70 potentiates illegitimate DNA doublestrand break repair and serves as a barrier to error-prone DNA repair pathways   [0145] 
Severe developmental defects, hypersensitivity to DNA-damaging agents, and lengthened telomeres in Arabidopsis MRE11 mutants   [0145] 
Repair pathway choices and consequences at the double strand break   [0145] 
Formation of the yeast Mre11-Rad50-Xrs2 complex is correlated with DNA repair and telomere maintenance   [0145] 
Xrcc1-dependent and Ku-dependent DNA double-strand break repair kinetics in Arabidopsis plants   [0145] 
Modernizing the nonhomologous end-joining repertoire: alternative and classical NHEJ share the stage   [0145] 
A glycine-arginine domain in control of the human MRE11 DNA repair protein   [0145] 
Ku80 plays a role in non homologous recombination but is not required for T-DNA integration in Arabidopsis   [0145] 
Disruption of the Arabidopsis RAD50 gene leads to plant sterility and MMS sensitivity   [0145] 
Genomic libraries and a host strain designed for highly efficient two-hybrid selection in yeast   [0145] 
Agrobacterium tumefaciens T-DNA integration and gene targeting in Arabidopsis thaliana non-homologous end-Joining mutants   [0145] 
Poly(ADP-ribose)polymerases are involved in microhomology mediated back-up non-homologous end joining in Arabidopsis thaliana   [0145] 
Multiple host-cell recombination pathways act in Agrobacterium mediated transformation of plant cells   [0145] 
A backup DNA repair pathway moves to the forefront   [0145] 
Crystal structure of human Mre11: Understanding tumorigenic mutations   [0145] 
Agrobacterium T-DNA integration into the plant genome can occur without the activity of key non-homologous end-joining proteins   [0145] 
Mre11 deficiency in Arabidopsis is associated with chromosomal instability in somatic cells and Spo11-dependent genome fragmentation during meiosis   [0145] 
Evidence for distinct functions of MRE11 in Arabidopsis meiosis   [0145] 
The MRE11 complex: starting from the ends   [0145] 
Identification of Ku70 and Ku80 homologues in Arabidopsis thaliana: evidence for a role in the repair of DNA double-strand breaks   [0145] 
VirB/D4-dependent protein translocation from Agrobacterium into plant cells   [0145] 
NBS1 is involved in DNA repair and plays a synergistic role with ATM in mediating meiotic homologous recombination in plants   [0145] 
An Arabidopsis Minute-like phenotype caused by a semi-dominant mutation in a RIBOSOMAL PROTEIN S5 gene   [0145] 
ABC ATPase signature helices in Rad50 link nucleotide state to Mre11 interface for DNA repair   [0145] 
DNA polymerase POLQ and cellular defense against DNA damage   [0145] 
The MRE11 GAR motif regulates DNA double-strand break processing and ATR activation   [0145] 
Mre11: roles in DNA repair beyond homologous recombination   [0145]